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Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy
INTRODUCTION: Degenerative myelopathy (DM) is a neurodegenerative spinal cord disease with upper motor neurons, with progressive and chronic clinical signs, similar to amyotrophic lateral sclerosis (ALS). DM has a complex etiology mainly associated with SOD1 gene mutation and its toxic role, with no...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374290/ https://www.ncbi.nlm.nih.gov/pubmed/37520009 http://dx.doi.org/10.3389/fvets.2023.1192744 |
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author | Gouveia, Débora Correia, Jéssica Cardoso, Ana Carvalho, Carla Oliveira, Ana Catarina Almeida, António Gamboa, Óscar Ribeiro, Lénio Branquinho, Mariana Sousa, Ana Lopes, Bruna Sousa, Patrícia Moreira, Alícia Coelho, André Rêma, Alexandra Alvites, Rui Ferreira, António Maurício, Ana Colette Martins, Ângela |
author_facet | Gouveia, Débora Correia, Jéssica Cardoso, Ana Carvalho, Carla Oliveira, Ana Catarina Almeida, António Gamboa, Óscar Ribeiro, Lénio Branquinho, Mariana Sousa, Ana Lopes, Bruna Sousa, Patrícia Moreira, Alícia Coelho, André Rêma, Alexandra Alvites, Rui Ferreira, António Maurício, Ana Colette Martins, Ângela |
author_sort | Gouveia, Débora |
collection | PubMed |
description | INTRODUCTION: Degenerative myelopathy (DM) is a neurodegenerative spinal cord disease with upper motor neurons, with progressive and chronic clinical signs, similar to amyotrophic lateral sclerosis (ALS). DM has a complex etiology mainly associated with SOD1 gene mutation and its toxic role, with no specific treatment. Daily intensive rehabilitation showed survival time near 8 months but most animals are euthanized 6–12 months after clinical signs onset. METHODS: This prospective controlled blinded cohort clinical study aims to evaluate the neural regeneration response ability of DM dogs subjected to an intensive neurorehabilitation protocol with mesenchymal stem cells (MSCs) transplantation. In total, 13 non-ambulatory (OFS 6 or 8) dogs with homozygous genotype DM/DM and diagnosed by exclusion were included. All were allocated to the intensive neurorehabilitation with MSCs protocol (INSCP) group (n = 8) or to the ambulatory rehabilitation protocol (ARP) group (n = 5), which differ in regard to training intensity, modalities frequency, and MSCs transplantation. The INSCP group was hospitalized for 1 month (T0 to T1), followed by MSCs transplantation (T1) and a second month (T2), whereas the ARP group was under ambulatory treatment for the same 2 months. RESULTS: Survival mean time of total population was 375 days, with 438 days for the INSCP group and 274 for the ARP group, with a marked difference on the Kaplan–Meier survival analysis. When comparing the literature's results, there was also a clear difference in the one-sample t-test (p = 0.013) with an increase in time of approximately 70%. OFS classifications between groups at each time point were significantly different (p = 0.008) by the one-way ANOVA and the independent sample t-test. DISCUSSION: This INSCP showed to be safe, feasible, and a possibility for a long progression of DM dogs with quality of life and functional improvement. This study should be continued. |
format | Online Article Text |
id | pubmed-10374290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103742902023-07-28 Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy Gouveia, Débora Correia, Jéssica Cardoso, Ana Carvalho, Carla Oliveira, Ana Catarina Almeida, António Gamboa, Óscar Ribeiro, Lénio Branquinho, Mariana Sousa, Ana Lopes, Bruna Sousa, Patrícia Moreira, Alícia Coelho, André Rêma, Alexandra Alvites, Rui Ferreira, António Maurício, Ana Colette Martins, Ângela Front Vet Sci Veterinary Science INTRODUCTION: Degenerative myelopathy (DM) is a neurodegenerative spinal cord disease with upper motor neurons, with progressive and chronic clinical signs, similar to amyotrophic lateral sclerosis (ALS). DM has a complex etiology mainly associated with SOD1 gene mutation and its toxic role, with no specific treatment. Daily intensive rehabilitation showed survival time near 8 months but most animals are euthanized 6–12 months after clinical signs onset. METHODS: This prospective controlled blinded cohort clinical study aims to evaluate the neural regeneration response ability of DM dogs subjected to an intensive neurorehabilitation protocol with mesenchymal stem cells (MSCs) transplantation. In total, 13 non-ambulatory (OFS 6 or 8) dogs with homozygous genotype DM/DM and diagnosed by exclusion were included. All were allocated to the intensive neurorehabilitation with MSCs protocol (INSCP) group (n = 8) or to the ambulatory rehabilitation protocol (ARP) group (n = 5), which differ in regard to training intensity, modalities frequency, and MSCs transplantation. The INSCP group was hospitalized for 1 month (T0 to T1), followed by MSCs transplantation (T1) and a second month (T2), whereas the ARP group was under ambulatory treatment for the same 2 months. RESULTS: Survival mean time of total population was 375 days, with 438 days for the INSCP group and 274 for the ARP group, with a marked difference on the Kaplan–Meier survival analysis. When comparing the literature's results, there was also a clear difference in the one-sample t-test (p = 0.013) with an increase in time of approximately 70%. OFS classifications between groups at each time point were significantly different (p = 0.008) by the one-way ANOVA and the independent sample t-test. DISCUSSION: This INSCP showed to be safe, feasible, and a possibility for a long progression of DM dogs with quality of life and functional improvement. This study should be continued. Frontiers Media S.A. 2023-07-13 /pmc/articles/PMC10374290/ /pubmed/37520009 http://dx.doi.org/10.3389/fvets.2023.1192744 Text en Copyright © 2023 Gouveia, Correia, Cardoso, Carvalho, Oliveira, Almeida, Gamboa, Ribeiro, Branquinho, Sousa, Lopes, Sousa, Moreira, Coelho, Rêma, Alvites, Ferreira, Maurício and Martins. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Veterinary Science Gouveia, Débora Correia, Jéssica Cardoso, Ana Carvalho, Carla Oliveira, Ana Catarina Almeida, António Gamboa, Óscar Ribeiro, Lénio Branquinho, Mariana Sousa, Ana Lopes, Bruna Sousa, Patrícia Moreira, Alícia Coelho, André Rêma, Alexandra Alvites, Rui Ferreira, António Maurício, Ana Colette Martins, Ângela Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy |
title | Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy |
title_full | Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy |
title_fullStr | Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy |
title_full_unstemmed | Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy |
title_short | Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy |
title_sort | intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy |
topic | Veterinary Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374290/ https://www.ncbi.nlm.nih.gov/pubmed/37520009 http://dx.doi.org/10.3389/fvets.2023.1192744 |
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